Canonical Allele Identifier: CA370038188
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187121T>C , CM000669.2:g.151187121T>C GRCh38
NC_000007.13:g.150884208T>C , CM000669.1:g.150884208T>C GRCh37
NC_000007.12:g.150515141T>C NCBI36
NG_017016.1:g.5712A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.10A>G MANE Select ENSP00000391137.2:p.Ser4Gly
ENST00000275838.5:c.10A>G ENSP00000275838.1:p.Ser4Gly
ENST00000377867.7:c.271+331A>G ENSP00000367098.3:n.271+331A>G
ENST00000415615.1:c.*122-68A>G ENSP00000410871.1:n.*122-68A>G
ENST00000420175.2:c.10A>G ENSP00000391137.2:p.Ser4Gly
NM_001142459.1:c.10A>G NP_001135931.2:p.Ser4Gly
NM_001142460.1:c.10A>G NP_001135932.2:p.Ser4Gly
NM_080871.3:c.271+331A>G NP_543147.2:n.271+331A>G
XM_005249949.3:c.145A>G XP_005250006.1:p.Ser49Gly
NM_001142459.2:c.10A>G MANE Select NP_001135931.2:p.Ser4Gly
NM_080871.4:c.271+331A>G NP_543147.2:n.271+331A>G